Production Supervisor Job at Beacon Hill (Noblesville, Indiana)

Production Supervisor

Beacon Hill

Location:
United States , Noblesville, Indiana

Category:
Manufacturing

Contract Type:
Employment contract

Salary:

92000.00 - 100000.00 USD / Year

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Job Description:

The Production Supervisor is responsible for the oversight of manufacturing operations associated with the manufacturing of radiopharmaceuticals, which meet approved specifications by supervising from the floor, coaching and developing their team, and ensuring that their area of operations maintains compliance with Corporate policies, local and federal regulations. The Supervisor is responsible for fostering a culture of team ownership, transparency, and team success.

Job Responsibility:

Ensure proper coverage of all production while also managing team PTO, trainings, absences, and other events impacting staffing
Ensure accountability, transparency, and effective communication cross-functionally and within the team
Review and approve weekly departmental schedules and maintenance activities
Ensure appropriate communication on production and project-related matters with area management
Coach and develop the team to high performance while fostering a culture of team ownership
Verify, review, and make appropriate changes if needed, to any controlled document pertinent to your area of responsibility
Ensure all employees comply with all policies, procedures, and site/company regulations
Set a clear vision by ensuring goals and objectives are aligned with site strategies through performance management
Exhibit accountability and responsibility for an area or process
Provide input on equipment installation, start-up, operation, and troubleshooting
Provide leadership for employee relations through effective communications, coaching, training and development
Supply the highest level of internal and external customer service
Lead and/or support all investigations, manufacturing exceptions, product failures, Root Cause Analyses, and customer complaints
Author, approve, and/or review all area quality and safety exceptions and investigation reports
Manage the department's overtime and ensure that all payroll exception reports are completed and submitted on time
Lead team in continuous improvement activities
Measure and communicate the team's progress against individual, team, site goals, and KPIs
Spend 70% of your time on the production floor directly with employees and processes
Must maintain operational compliance with US and international regulatory agencies and guidelines
Ensure all direct reports are properly trained
Conduct Production Team meetings as well as 1-on-1 coaching sessions with employees

Requirements:

Bachelor of Science degree in Manufacturing, Engineering, or related field required. Work experience is considered in lieu of a degree
Ten or more years of relevant work experience required, including experience in a cGMP environment, preferably in manufacturing
Two or more years of supervisory experience is required
Lean/Kaizen/Six Sigma experience preferred
Experience working with High Performance Teams
Coaching & Implementing Autonomous Maintenance activities preferred
Experience with developing/documenting procedures required
Aseptic and/or terminal sterilization processing experience preferred
Prior experience leading projects and/or being a core team member preferred

Nice to have:

Lean/Kaizen/Six Sigma experience
Coaching & Implementing Autonomous Maintenance activities
Aseptic and/or terminal sterilization processing experience
Prior experience leading projects and/or being a core team member

Additional Information:

Job Posted:
January 26, 2026

Employment Type:

Fulltime

Work Type:

On-site work

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